Antireflective articles and methods of making the same

ABSTRACT

A composite having (a) a substrate that has opposing first and second surfaces, the substrate being at least 90% transmissive in visible light and has less than 5% haze, (b) a nanostructured article including a matrix and a nanoscale dispersed phase and having a random nanostructured anisotropic surface; and (c) an optically clear adhesive disposed on the second surface of the substrate.

CROSS REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Application Ser.No. 61/141,517 filed on Dec. 30, 2008; Ser. No. 61/157,683 filed on Mar.5, 2009; and Ser. No. 61/234,782 filed Aug. 18, 2009, each of which isincorporated by reference in its entirety.

FIELD

This invention relates to nanostructured articles that are useful, forexample, as antireflective articles. In another aspect, this inventionrelates to methods for making nanostructured articles.

BACKGROUND

Whenever light travels from one medium to another, some portion of thelight is reflected from the interface between the two media. Forexample, about 4-5% of the light shining on a clear plastic substrate isreflected at the top surface.

Different approaches have been employed to reduce the reflection ofpolymeric materials. One approach is to use antireflective (AR) coatingssuch as multilayer reflective coatings consisting of transparent thinfilm structures with alternating layers of contrasting refractive indexto reduce reflection. It has proven difficult to achieve broadbandantireflection using AR coatings, however.

Another approach involves using subwavelength surface structure (forexample, subwavelength scale surface gratings) for broadbandantireflection. The methods for creating the subwavelength surfacestructure tend to be complicated and expensive batch processes, however.For example, the method disclosed in U.S. Patent Application PublicationNo. 2005/0233083 involves bombarding a polymeric surface with Ar/O₂plasma under vacuum conditions of less than 0.5 mTorr. This requirementof extreme vacuum conditions limits the commercial viability of themethod.

SUMMARY

In view of the foregoing, we recognize that there is a need foralternative approaches for reducing the reflection of surfaces,particularly polymeric surfaces. Furthermore, we recognize that in orderfor an approach for reducing the reflection of surfaces to commerciallyviable, it needs to be relatively simple and inexpensive.

Briefly, in one aspect, the present invention provides a nanostructuredarticle comprising a matrix and a nanoscale dispersed phase, and havinga random nanostructured anisotropic surface.

As used herein, “nanoscale” means submicron (for example, between about1 nm and about 500 nm); “nanostructured” means having one dimension onthe nanoscale; and “anisotropic surface” means a surface havingstructural asperities having a height to width (that is, average width)ratio of about 1.5:1 or greater (preferably, 2:1 or greater; morepreferably, 5:1 or greater).

The nanostructured articles of the invention exhibit a significantreduction in reflectance compared to an unstructured article comprisingthe same matrix material and nanodispersed phase. In addition, thenanostructured articles of the invention can be durable and possessscratch resistance. Some embodiments of the nanostructured articles ofthe invention also exhibit additional desirable properties such as, forexample, antifogging, easy cleaning, antimicrobial activity,hydrophilicity, or hydrophobicity.

In another aspect, the present disclosure provides methods of makingrandom nanostructured surfaces. One method comprises providing a matrixcomprising a nanodispersed phase, and anisotropically etching the matrixusing plasma to form a random nanostructured anisotropic surface.Another method comprises providing a matrix comprising a nanodispersedphase, and etching at least a portion of the nanodispersed phase usingplasma to form a random nanostructured surface.

In yet another aspect, the present disclosure provides a compositecomprising: (a) a substrate having at least 90% transmission in visiblelight and less than 5% haze, the substrate having opposing first andsecond surfaces; (b) a nanostructured article disposed on the firstsurface of the substrate, the nanostructured article comprising a matrixand a nanoscale dispersed phase, and having a random nanostructuredanisotropic surface; and (c) an optically clear adhesive disposed on thesecond surface of the substrate, the optically clear adhesive having atleast 90% transmission in visible light and less than 5% haze.

In yet another aspect, the present disclosure provides a method ofmaking a composite comprising the steps of: (a) providing a substratehaving at least 90% transmission in visible light and less than 5% haze;(b) coating a hardcoat composition on the first major surface of thesubstrate to yield a antireflective layer, the hardcoat compositioncomprising nanoparticles of SiO₂, ZrO₂ and combinations thereof, thenanoparticles dispersed in a matrix; (c) drying the hardcoat solution toyield an antireflective layer; (d) exposing the antireflective layer toreactive ion etching comprising the steps of (i) placing theantireflective layer on a cylindrical electrode in a vacuum vessel, (ii)introducing etchant gas to the vessel at a predetermined pressure, (iii)generating plasma between the cylindrical electrode and acounter-electrode; (iv) rotating the cylindrical electrode to translatethe substrate; and (v) anisotropically etching the hardcoat composition;and (e) laminating an optically clear adhesive disposed to the secondsurface of the substrate, the optically clear adhesive having at least90% transmission in visible light and less than 5% haze.

As used herein, “plasma” means a partially ionized gaseous or fluidstate of matter containing electrons, ions, neutral molecules, and freeradicals.

The methods of this disclosure can be carried out at moderate vacuumconditions (for example, between about 5 mTorr and about 10 mTorr). Theycan also be carried out as a roll-to-roll (that is, continuous) processusing cylindrical reactive ion etching (cylindrical RIE).

The present disclosure therefore meets the need in the art for ARsurfaces that are relatively simple and inexpensive to produce.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a first fragmentary perspective view of a coating apparatususeful in the present disclosure.

FIG. 2 is a second fragmentary perspective view of the apparatus of FIG.1 taken from a different vantage point.

FIG. 3 is a fragmentary perspective view of another embodiment of thecoating apparatus removed from its gas containing chamber.

FIG. 4 is a second perspective view of the apparatus of FIG. 3 takenfrom a different vantage point.

FIG. 5 is a scanning electron microscope photograph of an anisotropicnanostructured article of the disclosure.

FIG. 6 is a scanning electron microscope photograph of anotheranisotropic nanostructure article of the disclosure.

FIG. 7 is a schematic cross-sectional view of a display using theantireflective layer made according to one method of the presentdisclosure.

DETAILED DESCRIPTION

All numbers are herein assumed to be modified by the term “about.” Therecitation of numerical ranges by endpoints includes all numberssubsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3,3.80, 4, and 5). All parts recited herein are by weight unless otherwiseindicated.

The nanostructured articles comprise a matrix with a dispersed phase.The matrix (i.e., the continuous phase) can comprise polymeric material,liquid resins, inorganic material, or alloys or solid solutions(including miscible polymers).

In one aspect, the matrix includes a polymer selected from the groupconsisting of polycarbonate, poly(meth)acrylate, polyester, nylon,siloxane, fluoropolymer, urethane, epoxy, cyclic olefin copolymer,triacetate cellulose, diacrylate cellulose or blends or copolymersthereof.

Useful polymeric materials include thermoplastics and thermosettingresins. Suitable thermoplastics include, but are not limited to,polyethylene terephthalate (PET), polystyrene, acrylonitrile butadienestyrene, polyvinyl chloride, polyvinylidene chloride, polycarbonate,polyacrylates, thermoplastic polyurethanes, polyvinyl acetate,polyamide, polyimide, polypropylene, polyester, polyethylene,poly(methylmethacrylate), polyethylene naphthalate, styreneacrylonitrile, silicone-polyoxamide polymers, fluoropolymers, cyclicolefin copolymers, thermoplastic elastomers, and the like.

Suitable thermosetting resins include, but are not limited to, allylresin (including (meth)acrylates, polyester acrylates, urethaneacrylates, epoxy acrylates and polyether acrylates), epoxies,thermosetting polyurethanes, silicones or polysiloxanes, and the like.These resins can be formed from the reaction product of polymerizablecompositions comprising the corresponding monomers and or oligomers.

In one embodiment, the polymerizable compositions includes at least onemonomeric or oligomeric (meth)acrylate, preferably a urethane(meth)acrylate. Typically the monomeric or oligomeric (meth)acrylate ismulti(meth)acrylate. The term “(meth)acrylate” is used to designateesters of acrylic and methacrylic acids, and “multi(meth)acrylate”designates a molecule containing more than one (meth)acrylate group, asopposed to “poly(meth)acrylate” which commonly designates (meth)acrylatepolymers. Most often, the multi(meth)acrylate is a di(meth)acrylate, butit is also contemplated to employ tri(meth)acrylates,tetra(meth)acrylates and so on.

Suitable monomeric or oligomeric (meth)acrylates include alkyl(meth)acrylates such as methyl (meth)acrylate, ethyl (meth)acrylate,1-propyl (meth)acrylate and t-butyl (meth)acrylate. The acrylates mayinclude (fluoro)alkylester monomers of (meth)acrylic acid, the monomersbeing partially and or fully fluorinated, such as, trifluoroethyl(meth)acrylate.

Examples of commercially available multi(meth)acrylate resins includethe DIABEAM series from Mitsubishi Rayon Co., LTD.; the DINACOL seriesfrom Nagase & Company, Ltd.; the NK ESTER series from Shin-NakamuraChemical Co., Ltd.; the UNIDIC series from Dainippon Ink & Chemicals,Inc., the ARONIX series from Toagosei Co., LTD.; the BLENMER seriesmanufactured by NOF Corp.; the KAYARAD series from Nippon Kayaku Co.,Ltd., the LIGHT ESTER series and LIGHT ACRYLATE series from KyoeishaChemical Co., Ltd.

Oligomeric urethane multi(meth)acrylates may be obtained commercially,for example from Sartomer under the trade designation “Photomer 6000Series”, such as “Photomer 6010” and “Photomer 6020”, and also under thetrade designation “CN 900 Series”, such as “CN966B85”, “CN964” and“CN972”. Oligomeric urethane (meth)acrylates are also available fromSurface Specialties, such as available under the trade designations“Ebecryl 8402”, “Ebecryl 8807” and “Ebecryl 4827”. Oligomeric urethane(meth)acrylates may also be prepared by the initial reaction of analkylene or aromatic diisocyanate of the formula OCN—R₃—NCO with apolyol. Most often, the polyol is a diol of the formula HO—R₄—OH whereR₃ is a C2-100 alkylene or an arylene group and R₄ is a C2-100 alkylenegroup. The intermediate product is then a urethane diol diisocyanate,which subsequently can undergo reaction with a hydroxyalkyl(meth)acrylate. Suitable diisocyanates include 2,2,4-trimethylhexylenediisocyanate and toluene diisocyanate. Alkylene diisocyanates aregenerally preferred. A particularly preferred compound of this type maybe prepared from 2,2,4-trimethylhexylene diisocyanate,poly(caprolactone)diol and 2-hydroxyethyl methacrylate. In at least somecases, the urethane (meth)acrylate is preferably aliphatic.

The polymerizable compositions can be mixtures of various monomers andor oligomers, having the same or differing reactive functional groups.Polymerizable compositions comprising two or more different functionalgroups may be used, including the following; (meth)acrylate, epoxy andurethane. The differing functionality may be contained in differentmonomeric and or oligomeric moieties or in the same monomeric and oroligomeric moiety. For example, a resin composition may comprise anacrylic or urethane resin having an epoxy group and or a hydroxyl groupin the side chain, a compound having an amino group and, optionally, asilane compound having an epoxy group or amino group in the molecule.

The thermosetting resin compositions are polymerizable usingconventional techniques such as thermal cure, photocure (cure by actinicradiation) and or e-beam cure. In one embodiment, the resin isphotopolymerized by exposing it to ultraviolet (UV) and or visiblelight. Conventional curatives and or catalyst may be used in thepolymerizable compositions and are selected based on the functionalgroup(s) in the composition. Multiple curatives and or catalysts may berequired if multiple cure functionality is being used. Combining one ormore cure techniques, such as thermal cure, photocure and e-beam cure,is within the scope of the present disclosure.

Furthermore, the polymerizable resins can be compositions comprising atleast one other monomer and or oligomer (that is, other than thosedescribed above, namely the monomeric or oligomeric (meth)acrylate andthe oligomeric urethane (meth)acrylate). This other monomer may reduceviscosity and/or improve thermomechanical properties and/or increaserefractive index. Monomers having these properties include acrylicmonomers (that is, acrylate and methacrylate esters, acrylamides andmethacrylamides), styrene monomers and ethylenically unsaturatednitrogen heterocycles.

Also included are (meth)acrylate esters having other functionality.Compounds of this type are illustrated by the 2-(N-butylcarbamyl)ethyl(meth)acrylates, 2,4-dichlorophenyl acrylate, 2,4,6-tribromophenylacrylate, tribromophenoxylethyl acrylate, t-butylphenyl acrylate, phenylacrylate, phenyl thioacrylate, phenylthioethyl acrylate, alkoxylatedphenyl acrylate, isobornyl acrylate and phenoxyethyl acrylate. Thereaction product of tetrabromobisphenol A diepoxide and (meth)acrylicacid is also suitable.

The other monomer may also be a monomeric N-substituted orN,N-disubstituted (meth)acrylamide, especially an acrylamide. Theseinclude N-alkylacrylamides and N,N-dialkylacrylamides, especially thosecontaining C1-4 alkyl groups. Examples are N-isopropylacrylamide,N-t-butylacrylamide, N,N-dimethylacrylamide and N,N-diethylacrylamide.

The other monomer may further be a polyol multi(meth)acrylate. Suchcompounds are typically prepared from aliphatic diols, triols, and/ortetraols containing 2-10 carbon atoms. Examples of suitablepoly(meth)acrylates are ethylene glycol diacrylate, 1,6-hexanedioldiacrylate, 2-ethyl-2-hydroxymethyl-1,3-propanediol triacylate(trimethylolpropane triacrylate), di(trimethylolpropane) tetraacrylate,pentaerythritol tetraacrylate, the corresponding methacrylates and the(meth)acrylates of alkoxylated (usually ethoxylated) derivatives of saidpolyols. Monomers having two or more (ethylenically unsaturated groupscan serve as a crosslinker.

Styrenic compounds suitable for use as the other monomer includestyrene, dichlorostyrene, 2,4,6-trichlorostyrene, 2,4,6-tribromostyrene,4-methylstyrene and 4-phenoxystyrene. Ethylenically unsaturated nitrogenheterocycles include N-vinylpyrrolidone and vinylpyridine.

Constituent proportions in the radiation curable materials can vary. Ingeneral, the organic component can comprise about 30-100% monomeric andor oligomeric (meth)acrylate or oligomeric urethane multi(meth)acrylate,with any balance being the other monomer and or oligomer.

Commercially available liquid-resin based materials (typically referredto as “hardcoats”) may be used as the matrix or as a component of thematrix. Such materials include the PERMANEW series from CaliforniaHardcoating Co., San Diego, Calif. and the UVHC series harcoats fromMomentive Performance Materials, Albany, N.Y. Additionally, commerciallyavailable nanoparticle filled matrix may be used, such as NANOCRYL andNANOPDX from Nanoresins AG, Geesthacht Germany.

Additionally, nanoparticulate containing hardcoat films, such as THSseries from Toray Advanced Films Co., Ltd., Tokyo, Japan; the OpteriaHardcoated Films for FPD from Lintec Corp., Tokyo, Japan; the SonyOptical Film from Sony Chemical & Device Corp., Tokyo, JP; theHardcoated Film from SKC Haas, Seoul, Korea and the Terrappin G filmfrom Tekra Corp., Milwaukee, Wis., may be used as the matrix or acomponent of the matrix.

Surface leveling agents may be added to the matrix. The leveling agentis preferably used for smoothing the matrix resin. Examples includesilicone-leveling agents, acrylic-leveling agents andfluorine-containing-leveling agents. In one embodiment, thesilicone-leveling agent includes a polydimethyl siloxane backbone towhich polyoxyalkylene groups are added.

Useful inorganic materials for the matrix include, for example, glasses,metals, metal oxides, and ceramics. Preferred inorganic materialsinclude silicon oxide, zirconia, vanadium pentoxide, and tungstencarbide.

The nanoscale dispersed phase is a discontinuous phase randomlydispersed within the matrix. The nanoscale dispersed phase can comprisenanoparticles (for example, nanospheres), nanotubes, nanofibers, cagedmolecules, hyperbranched molecules, micelles, reverse micelles, or thelike. Preferably, the dispersed phase comprises nanoparticles or cagedmolecules; more preferably, the dispersed phase comprises nanoparticles.

Nanoparticles preferably have a mean diameter in the range from about 1nm to about 100 nm. Preferably, the nanoparticles have a mean diameterof 5 nm, 20 nm, or 80 nm. Nanoparticles for the dispersed phase cancomprise metals, metal oxides, carbides, nitrides, borides, halides,fluorocarbon solids, or the like, or mixtures thereof. Preferredmaterials include SiO₂, ZrO₂, TiO₂, ZnO, calcium carbonate, magnesiumsilicate, indium tin oxide, antimony tin oxide, carbon,poly(tetrafluoroethylene), and the like. Preferably, the nanoparticlescomprise SiO₂.

Nanoparticles can be present in the matrix in an amount from about 1% toabout 60%, or about 10% to about 40% by weight. Silicas for use in thematerials of the present disclosure are commercially available fromNalco Chemical Co., Naperville, Ill. under the trade designation “NalcoColloidal Silicas” such as products 1040, 1042, 1050, 1060, 2327 and2329. Suitable fumed silicas include for example, products commerciallyavailable from Evonik under the trade designation, “Aerosil seriesOX-50”, as well as product numbers -130, -150, and -200. Other colloidalsilica can be also obtained from Nissan Chemicals under the designations“IPA-ST”, “IPA-ST-L”, and “IPA-ST-ML”. Fumed silicas are alsocommercially available from Cabot Corp., Tuscola, Ill., under thedesignations “CAB-O-SPERSE 2095”, “CAB-O-SPERSE A105”, and “CAB-O-SILM5”. Zirconias for use in composition and articles of the invention areavailable from Nalco Chemical Co. under the trade designation “NalcoOOSSOO8”.

Surface-treating the nano-sized particles can provide a stabledispersion in the polymeric resin. Preferably, the surface-treatmentstabilizes the nanoparticles so that the particles will be welldispersed in the polymerizable resin and result in a substantiallyhomogeneous composition. Furthermore, the nanoparticles can be modifiedover at least a portion of its surface with a surface treatment agent sothat the stabilized particles can copolymerize or react with thepolymerizable resin during curing.

The nanoparticles are preferably treated with a surface treatment agent.In general, a surface treatment agent has a first end that will attachto the particle surface (covalently, ionically or through strongphysisorption) and a second end that imparts compatibility of theparticle with the resin and/or reacts with resin during curing. Examplesof surface treatment agents include alcohols, amines, carboxylic acids,sulfonic acids, phosphonic acids, silanes and titanates. The preferredtype of treatment agent is determined, in part, by the chemical natureof the metal oxide surface. Silanes are preferred for silica and otherfor siliceous fillers. Silanes and carboxylic acids are preferred formetal oxides such as zirconia. The surface modification can be doneeither subsequent to mixing with the monomers or after mixing. It ispreferred in the case of silanes to react the silanes with the particlesor nanoparticle surface before incorporation into the resins. Therequired amount of surface modifier is dependant on several factors suchas particle size, particle type, molecular weight of the modifier, andmodifier type.

Representative embodiments of surface treatment agents include compoundssuch as, for example, isooctyl tri-methoxy-silane,N-(3-triethoxysilylpropyl)methoxyethoxyethoxyethyl carbamate (PEG3TES),N-(3-triethoxysilylpropyl)methoxyethoxyethoxyethyl carbamate (PEG2TES),3-(methacryloyloxy)propyltrimethoxysilane,3-acryloxypropyltrimethoxysilane,3-(methacryloyloxy)propyltriethoxysilane,3-(methacryloyloxy)propylmethyldimethoxysilane,3-(acryloyloxypropyl)methyldimethoxysilane,3-(methacryloyloxy)propyldimethylethoxysilane,vinyldimethylethoxysilane, pheyltrimethaoxysilane,n-octyltrimethoxysilane, dodecyltrimethoxysilane,octadecyltrimethoxysilane, propyltrimethoxysilane,hexyltrimethoxysilane, vinylmethyldiactoxysilane,vinylmethyldiethoxysilane, vinyltriacetoxysilane, vinyltriethoxysilane,vinyltriisopropoxysilane, vinyltrimethoxysilane, vinyltriphenoxysilane,vinyltri-t-butoxysilane, vinyltris-isobutoxysilane,vinyltriisopropenoxysilane, vinyltris(2-methoxyethoxy)silane,styrylethyltrimethoxysilane, mercaptopropyltrimethoxysilane,3-glycidoxypropyltrimethoxysilane, acrylic acid, methacrylic acid, oleicacid, stearic acid, dodecanoic acid, 2-(2-(2-methoxyethoxy)ethoxy)aceticacid (MEEAA), beta-carboxyethylacrylate, 2-(2-methoxyethoxy)acetic acid,methoxyphenyl acetic acid, and mixtures thereof. Furthermore, aproprietary silane surface modifier, commercially available from OSISpecialties, Crompton South Charleston, W. Va., under the tradedesignation “Silquest A1230” is also suitable.

The surface modification of the particles in the colloidal dispersioncan be accomplished in a variety of ways. The process involves themixture of an inorganic dispersion with surface modifying agents.Optionally, a co-solvent can be added at this point, such as forexamples, 1-methoxy-2-propanol, ethanol, isopropanol, ethylene glycol,N,N-dimethylacetamide and 1-methyl-2-pyrrolidinone. The co-solvent canenhance the solubility of the surface modifying agents as well as thesurface modified particles. The mixture comprising the inorganic sol andsurface modifying agents is subsequently reacted at room or an elevatedtemperature, with or without mixing. In one method, the mixture can bereacted at about 85° C. for about 24 hours, resulting in the surfacemodified sol. In another method, where metal oxides are surface modifiedthe surface treatment of the metal oxide can preferably involve theadsorption of acidic molecules to the particle surface. The surfacemodification of the heavy metal oxide preferably takes place at roomtemperature.

The surface modification of ZrO₂ with silanes can be accomplished underacidic conditions or basic conditions. In one case the silanes areheated under acid conditions for a suitable period of time. At whichtime the dispersion is combined with aqueous ammonia (or other base).This method allows removal of the acid counter ion from the ZrO₂ surfaceas well as reaction with the silane. In another method the particles areprecipitated from the dispersion and separated from the liquid phase.

A combination of surface modifying agents can be useful, wherein atleast one of the agents has a functional group co-polymerizable with ahardenable resin. For example, the polymerizing group can beethylenically unsaturated or a cyclic function subject to ring openingpolymerization. An ethylenically unsaturated polymerizing group can be,for example, an acrylate or methacrylate, or vinyl group. A cyclicfunctional group subject to ring opening polymerization generallycontains a heteroatom such as oxygen, sulfur or nitrogen, and preferablya 3-membered ring containing oxygen such as an epoxide.

Useful caged molecules for the nanodispersed phase include polyhedraloligomeric silsesquioxane molecules, which are cage-like hybridmolecules of silicone and oxygen. Polyhedral oligomeric silsesquioxane(POSS) molecules are derived from a continually evolving class ofcompounds closely related to silicones through both composition and ashared system of nomenclature. POSS molecules have two unique features(1) the chemical composition is a hybrid, intermediate (RSiO_(1.5))between that of silica (SiO₂) and silicone (R₂SiO), and (2) themolecules are physically large with respect to polymer dimensions andnearly equivalent in size to most polymer segments and coils.Consequently, POSS molecules can be thought of as the smallest particles(about 1-1.5 nm) of silica possible. However unlike silica or modifiedclays, each POSS molecule contains covalently bonded reactivefunctionalities suitable for polymerization or grafting POSS monomers topolymer chains. In addition, POSS acrylate and methacrylate monomers aresuitable for ultraviolet (UV) curing. High functionality POSS acrylatesand methacrylates (for example, MA0735 and MA0736) are miscible withmost of the UV-curable acrylic and urethane acrylic monomers oroligomers to form mechanically durable hardcoat in which POSS moleculesform nano-phases uniformly dispersed in the organic coating matrix.

Carbon can also be used in the nanodispersed phase in the form ofgraphite, carbon nanotubes, bulky balls, or carbon black such asdescribed in U.S. Pat. No. 7,368,161 (McGurran et al.).

Additional materials that can be used in the nanodispersed phase includeIrgastat™ P18 (available from Ciba Corporation, Tarrytown, N.Y.) andAmpacet LR-92967 (available from Ampacet Corporation, Tarrytown, N.Y.).

The dispersed phase is typically present in the matrix at concentrationsbetween about 1 weight % and about 50 weight %; preferably between about5 weight % and about 25 weight %.

The nanostructured articles of the invention have a nanostructuredanisotropic surface. The nanostructured anisotropic surface typicallycomprises nanofeatures having a height to width ratio of about 2:1 orgreater; preferably about 5:1 or greater. In some embodiments, theheight to width ratio is even 50:1 or greater, 100:1 or greater, or200:1 or greater. The nanostructured anisotropic surface can comprisenanofeatures such as, for example, nano-pillars or nano-columns, orcontinuous nano-walls comprising nano-pillars or nano-columns.Preferably, the nanofeatures have steep side walls that are roughlyperpendicular to the substrate. In some embodiments, the majority of thenanofeatures are capped with dispersed phase material. The concentrationof the dispersed phase at the surface (versus in the interior of thematrix) can be between about 5 weight % and about 90 weight %;preferably between about 10 weight % and about 75 weight %. In someembodiments, the concentration of the dispersed phase is higher at thesurface of the matrix than within the matrix.

In some embodiments the matrix may comprise materials for staticdissipation in order to minimize attraction of dirt and particulate andthus maintain surface quality. Suitable materials for static dissipationinclude, for example, Stat-Rite™ polymers such X-5091, M-809, S-5530,S-400, S-403, and S-680 (available from Lubrizol, Wickliffe, Ohio);3,4-polyethylenedioxythiophene-polystyrenesulfonate (PEDOT/PSS)(available from H.C. Starck, Cincinnati, Ohio); polyanaline;polythiophene; Pelestat™ NC6321 and NC7530 antistatic additives(available from Tomen America Inc., New York, N.Y.); antistaticcompositions containing at least one ionic salt consisting of anonpolymeric nitrogen onium cation and a weakly coordinatingfluororganic anion as disclosed in U.S. Pat. No. 6,372,829 and asdisclosed in U.S. Patent Application Publication 2007/0141329 A1.

The nanostructured surface is formed by anisotropically etching thematrix. The matrix comprising the nanoscale dispersed phase can beprovided, for example, as a coating on a substrate. The substrate canbe, for example, a polymeric substrate, a glass substrate or window, ora function device such as an organic light emitting diode (OLED), adisplay, a photovoltaic device, or the like. The matrix comprising thedispersed phase can be coated on the substrate and cured using methodsknown in the art such as, for example, casting cure by casting drum, diecoating, flow coating, or dip coating. The coating can be prepared inany desired thickness greater than about 1 micron or preferably greaterthan about 4 microns. In addition the coating can be cured by UV,electron beam, or heat. Alternatively, the matrix comprising thedispersed phase may be the article itself.

In some embodiments, the surface of the matrix comprising the nanoscaledispersed phase may be microstructured. For example, a substrate with av-groove microstructured surface can be coated with polymerizable matrixmaterials comprising a nanodispersed phase and treated by plasma etchingto form nanostructures on v-groove microstructured surface.Alternatively, a microstructured article such as Fresnel lens or amicrostructured article comprising microreplicated posts or columnscomprising nanodispersed phases can be also treated by plasma etching toform nanostructures on microstructures. Other examples include a finemicro-structured surface resulting from controlling the solventevaporation process from multi-solvent coating solutions, described asin U.S. Pat. No. 7,378,136; or the structured surface from themicro-replication method disclosed in U.S. Pat. No. 7,604,381; or anyother structured surface induced by electrical and magnetic field orother means.

The matrix is anisotropically etched using chemically reactive plasma.The RIE process, for example, involves generating plasma under vacuum byan electromagnetic field. High energy ions from the plasma attack oretch away the matrix material.

A typical RIE system consists of a vacuum chamber with two parallelelectrodes, the “powered electrode” (or “sample carrier electrode”) andthe counter-electrode, which create an electric field that acceleratesions toward. The powered electrode is situated in the bottom portion ofthe chamber and is electrically isolated from the rest of the chamber.The article or sample to be nanostructured is placed on the poweredelectrode. Reactive gas species can be added to the chamber, forexample, through small inlets in the top of the chamber and can exit tothe vacuum pump system at the bottom of the chamber. Plasma is formed inthe system by applying a RF electromagnetic field to the poweredelectrode. The field is typically produced using a 13.56 MHz oscillator,although other RF sources and frequency ranges may be used. The gasmolecules are broken and can become ionized in the plasma andaccelerated toward the powered electrode to etch the sample. The largevoltage difference causes the ions to be directed toward the poweredelectrode where they collide with the sample to be etched. Due to themostly vertical delivery of the ions, the etch profile of the sample issubstantially anisotropic. Preferably, the powered electrode is smallerthan the counter-electrode creating a large voltage potential across theion sheath adjacent the powered electrode. Preferably, the etching is toa depth greater than about 100 nm.

The process pressure is typically maintained at below about 20 mTorr(preferably, below about 10 mTorr) but greater than about 1 mTorr. Thispressure range is very conducive for generation of the anisotropicnanostructure in a cost effective manner. When the pressure is aboveabout 20 mTorr, the etching process becomes more isotropic because ofthe collisional quenching of the ion energy. Similarly, when thepressure goes below about 1 mTorr, the etching rate becomes very lowbecause of the decrease in number density of the reactive species. Also,the gas pumping requirements become very high.

The power density of the RF power of the etching process is preferablyin the range of about 0.1 to about 1.0 watts/cm³ (preferably, about 0.2to about 0.3 watts/cm³).

The type and amount of gas utilized will depend upon the matrix materialto be etched. The reactive gas species need to selectively etch thematrix material rather than the dispersed phase. Additional gases may beused for enhancing the etching rate of hydrocarbons or for the etchingof non-hydrocarbon materials. For example, fluorine containing gasessuch as perfluoromethane, perfluoroethane, perfluoropropane,sulfurhexafluoride, nitrogen trifluoride, and the like can be added tooxygen or introduced by themselves to etch materials such as SiO₂,tungsten carbide, silicon nitride, amorphous silicon, and the like.Chlorine-containing gases can likewise be added for the etching ofmaterials such as aluminum, sulfur, boron carbide, and semiconductorsfrom the Group II-VI (including, but not limited to, cadmium, magnesium,zinc, sulfur, selenium, tellurium, and combinations thereof and from theGroup III-V (including, but not limited to, aluminum, gallium, indium,arsenic, phosphorous, nitrogen, antimony, or combinations thereof.Hydrocarbon gases such as methane can be used for the etching ofmaterials such as gallium arsenide, gallium, indium, and the like. Inertgases, particularly heavy gases such as argon can be added to enhancethe anisotropic etching process.

Advantageously, the method of the invention can also be carried outusing a continuous roll-to-roll process. For example, the method of theinvention can be carried out using “cylindrical” RIE. Cylindrical RIEutilizes a rotating cylindrical electrode to provide anisotropicallyetched nanostructures on the surface of the articles of the invention.

In general, cylindrical RIE for making the nanostructured articles ofthe invention can be described as follows. A rotatable cylindricalelectrode (“drum electrode”) powered by radio-frequency (RF) and agrounded counter-electrode are provided inside a vacuum vessel. Thecounter-electrode can comprise the vacuum vessel itself. Gas comprisingan etchant is fed into the vacuum vessel, and plasma is ignited andsustained between the drum electrode and the grounded counter-electrode.The conditions are selected so that sufficient ion bombardment isdirected perpendicular to the circumference of the drum. A continuousarticle comprising the matrix containing the nanodispersed phase canthen be wrapped around the circumference of the drum and the matrix canbe etched in the direction normal to the plane of the article. Thematrix can be in the form of a coating on an article such as, forexample, on a film or web, or the matrix can be the article itself. Theexposure time of the article can be controlled to obtain a predeterminedetch depth of the resulting nanostructure. The process can be carriedout at an operating pressure of approximately 10 mTorr.

FIGS. 1 and 2 illustrate a cylindrical RIE apparatus that is useful forthe methods of the invention. A common element for plasma creation andion acceleration is generally indicated as 10. This RIE apparatus 10includes a support structure 12, a housing 14 including a front panel 16of one or more doors 18, side walls 20 and a back plate 22 defining aninner chamber 24 therein divided into one or more compartments, a drum26 rotatably affixed within the chamber, a plurality of reel mechanismsrotatably affixed within the chamber and referred to generally as 28,drive mechanism 37 for rotatably driving drum 26, idler rollers 32rotatably affixed within the chamber, and vacuum pump 34 fluidlyconnected to the chamber.

Support structure 12 is any means known in the art for supportinghousing 14 in a desired configuration, a vertically upright manner inthe present case. As shown in FIGS. 1 and 2, housing 14 can be atwo-part housing as described below in more detail. In this embodiment,support structure 12 includes cross supports 40 attached to each side ofthe two-part housing for supporting apparatus 10. Specifically, crosssupports 40 include both wheels 42 and adjustable feet 44 for moving andsupporting, respectively, apparatus 10. In the embodiment shown in FIGS.1 and 2, cross supports 40 are attached to each side of housing 14through attachment supports 46. Specifically, cross supports 40 areconnected to one of side wails 20, namely the bottom side wall, viaattachment supports 46, while cross supports 40 on the other side ofhousing 14 are connected to back plate 22 by attachment supports 46. Anadditional crossbar 47 is supplied between cross supports 40 on theright-hand side of apparatus 10 as shown in FIG. 1. This can provideadditional structural reinforcement.

Housing 14 can be any means of providing a controlled environment thatis capable of evacuation, containment of gas introduced afterevacuation, plasma creation from the gas, ion acceleration, and etching.In the embodiment shown in FIGS. 1 and 2, housing 14 has outer wallsthat include front panel 16, four side walls 20, and a back plate 22.The outer walls define a box with a hollow interior, denoted as chamber24. Side walls 20 and back plate 22 are fastened together, in any mannerknown in the art, to rigidly secure side walls 20 and back plate 22 toone another in a manner sufficient to allow for evacuation of chamber24, containment of a fluid for plasma creation, plasma creation, ionacceleration, and etching. Front panel 16 is not fixedly secured so asto provide access to chamber 24 to load and unload substrate materialsand to perform maintenance. Front panel 16 is divided into two platesconnected via hinges 50 (or an equivalent connection means) to one ofside walls 20 to define a pair of doors 18. These doors seal to the edgeof side walls 20, preferably through the use of a vacuum seal (forexample, an O-ring). Locking mechanisms 52 selectively secure doors 18to side walls 20 and can be any mechanism capable of securing doors 18to walls 20 in a manner allowing for evacuation of chamber 24, storageof a fluid for plasma creation, plasma creation, ion acceleration, andetching.

In one embodiment, chamber 24 is divided by a divider wall 54 into twocompartments 56 and 58. A passage or hole 60 in wall 54 provides forpassage of fluids or substrate between compartments. Alternatively, thechamber can be only one compartment or three or more compartments.Preferably, the chamber is only one compartment.

Housing 14 includes a plurality of view ports 62 with high pressure,clear polymeric plates 64 sealably covering ports 62 to allow forviewing of the etching process occurring therein. Housing 14 alsoincludes a plurality of sensor ports 66 in which various sensors (forexample, temperature, pressure, etc.) can be secured. Housing 14 furtherincludes inlet ports 68 providing for conduit connection through whichfluid can be introduced into chamber 24 as needed. Housing 14 alsoincludes pump ports 70 and 72 that allow gases and liquids to be pumpedor otherwise evacuated from chamber 24.

Pump 34 is shown suspended from one of sides 20, preferably the bottom(as shown in FIG. 2). Pump 34 can be, for example, a turbo-molecularpump fluidly connected to the controlled environment within housing 14.Other pumps, such as diffusion pumps or cryopumps, can be used toevacuate lower chamber 58 and to maintain operating pressure therein.The process pressure during the etching step is preferably chosen to bebetween about 1 mTorr and about 20 mTorr to provide anisotropic etching.Sliding valve 73 is positioned along this fluid connection and canselectively intersect or block fluid communication between pump 34 andthe interior of housing 14. Sliding valve 73 is movable over pump port62 so that pump port 62 can be fully open, partially open, or closedwith respect to fluid communication with pump 34.

Drum 26 preferably is a cylindrical electrode 80 with an annular surface82 and two planar end surfaces 84. The electrode can be made of anyelectrically conductive material and preferably is a metal such as, forexample, aluminum, copper, steel, stainless steel, silver, chromium oran alloy of any one or more of the foregoing. Preferably, the electrodeis aluminum, because of the ease of fabrication, low sputter yield, andlow costs.

Drum 26 is further constructed to include non-coated, conductive regionsthat allow an electric field to permeate outward as well asnon-conductive, insulative regions for preventing electric fieldpermeation and thus for limiting film coating to the non-insulated orconductive portions of the electrode. The electrically non-conductivematerial typically is an insulator, such as a polymer (for example,polytetrafluoroethylene). Various embodiments that fulfill thiselectrically non-conductive purpose so as to provide only a smallchannel, typically the width of the substrate to be coated, as aconductive area can be envisioned by one of ordinary skill in the art.

FIG. 1 shows an embodiment of drum 26 where annular surface 82 and endsurfaces 84 of drum 26 are coated with an electrically non-conductive orinsulative material, except for annular channel 90 in annular surface 82which remains uncoated and thus electrically conductive. In addition, apair of dark space shields 86 and 88 cover the insulative material onannular surface 82, and in some embodiments cover end surfaces 84. Theinsulative material limits the surface area of the electrode along whichplasma creation and negative biasing may occur. However, since theinsulative materials sometimes can become fouled by the ion bombardment,dark space shields 86 and 88 can cover part or all of the insulatedmaterial. These dark space shields may be made from a metal such asaluminum but do not act as conductive agents because they are separatedfrom the electrode by means of an insulating material (not shown). Thisallows confinement of the plasma to the electrode area.

Another embodiment of drum 26 is shown in FIGS. 3 and 4 where drum 26includes a pair of insulative rings 85 and 87 affixed to annular surface82 of drum 26. In some embodiments, insulative ring 87 is a cap whichacts to also cover end surface 84. Bolts 92 secure support means 94,embodied as a flat plate or strap, to back plate 22. Bolts 92 andsupport means 94 can assist in supporting the various parts of drum 26.The pair of insulative rings 85 and 87, once affixed to annular surface82, define an exposed electrode portion embodied as channel 90.

In any case, electrode 80 is covered in some manner by an insulativematerial in all areas except where the substrate contacts the electrode(that is, touching or within the plasma dark space limit of theelectrode (for example, about 3 mm)). This defines an exposed electrodeportion that can be in intimate contact with the substrate. Theremainder of the electrode is covered by an insulative material. Whenthe electrode is powered and the electrode becomes negatively biasedwith respect to the resultant plasma, this relatively thick insulativematerial prevents etching on the surfaces it covers. As a result,etching is limited to the uncovered area (that is, that which is notcovered with insulative material, channel 90), which preferably iscovered by relatively thin substrate material.

Referring to FIGS. 1 and 2, drum 26 is rotatably affixed to back plate22 through a ferrofluidic feedthrough and rotary union 38 (or anequivalent mechanism) affixed within a hole in back plate 22. Theferrofluidic feedthrough and rotary union provide separate fluid andelectrical connection from a standard coolant fluid conduit andelectrical wire to hollow coolant passages and the conductive electrode,respectively, of rotatable drum 26 during rotation while retaining avacuum seal. The rotary union also supplies the necessary force torotate the drum, which force is supplied from any drive means such as abrushless DC servo motor. However, connection of drum 26 to back plate22 and the conduit and wire may be performed by any means capable ofsupplying such a connection and is not limited to a ferrofluidicfeedthrough and a rotary union. One example of such a ferrofluidicfeedthrough and rotary union is a two-inch (about 5 cm) inner diameterhollow shaft feedthrough made by Ferrofluidics Co. (Nashua, N.H.).

Drum 26 is rotatably driven by drive assembly 37, which can be anymechanical and/or electrical system capable of translating rotationalmotion to drum 26. In the embodiment shown in FIG. 2, drive assembly 37includes motor 33 with a drive shaft terminating in drive pulley 31 thatis mechanically connected to a driven pulley 39 rigidly connected todrum 26. Belt 35 (or equivalent structure) translates rotational motionfrom drive pulley 31 to driven pulley 39.

The plurality of reel mechanisms 28 are rotatably affixed to back plate22. The plurality of reel mechanisms 28 includes a substrate reelmechanism with a pair of substrate spools 28A and 28B, and, in someembodiments, also can include a spacing web reel mechanism with a pairof spacing web spools 28C and 28D, and masking web reel mechanism with apair of masking web spools 28E and 28F, where each pair includes onedelivery and one take-up spool. As is apparent from FIG. 2, at leasteach take-up reel 28B, 28D, and 28F includes a drive mechanism 27mechanically connected thereto such as a standard motor as describedbelow for supplying a rotational force that selectively rotates the reelas needed during etching. In addition, each delivery reel 28A, 28C, and28E in select embodiments includes a tensioner for supplying tautness tothe webs and/or a drive mechanism 29.

Each reel mechanism includes a delivery and a take-up spool which may bein the same or a different compartment from each other, which in turnmay or may not be the same compartment the electrode is in. Each spoolis of a standard construction with an axial rod and a rim radiallyextending from each end defining a groove in which an elongated member,in this case a substrate or web, is wrapped or wound. Each spool issecurably affixed to a rotatable stem sealably extending through backplate 22. In the case of spools to be driven, the stem is mechanicallyconnected to a motor 27 (for example, a brushless DC servo motor). Inthe case of non-driven spools, the spool is merely coupled in arotatable manner through a coupling 29 to back plate 22 and may includea tension mechanism to prevent slack.

RIE apparatus 10 also includes idler rollers 32 rotatably affixed withinthe chamber and pump 34 fluidly connected to the chamber. The idlerrollers guide the substrate from the substrate spool 28A to channel 90on drum 26 and from channel 90 to take-up substrate spool 28B. Inaddition, where spacing webs and masking webs are used, idler rollers 32guide these webs and the substrate from substrate spool 28A and maskingweb spool 28E to channel 90 and from channel 90 to take-up substratespool 28B and take-up masking web spool 28F, respectively.

RIE apparatus 10 further includes a temperature control system forsupplying temperature controlling fluid to electrode 80 via ferrofluidicfeedthrough 38. The temperature control system may be provided onapparatus 10 or alternatively may be provided from a separate system andpumped to apparatus 10 via conduits so long as the temperature controlfluid is in fluid connection with passages within electrode 80. Thetemperature control system may heat or cool electrode 80 as is needed tosupply an electrode of the proper temperature for etching. In apreferred embodiment, the temperature control system is a coolant systemusing a coolant such as, for example, water, ethylene glycol, chlorofluorocarbons, hydrofluoroethers, and liquefied gases (for example,liquid nitrogen).

RIE apparatus 10 also includes an evacuation pump fluidly connected toevacuation port(s) 70. This pump may be any vacuum pump, such as a Rootsblower, a turbo molecular pump, a diffusion pump, or a cryopump, capableof evacuating the chamber. In addition, this pump may be assisted orbacked up by a mechanical pump. The evacuation pump may be provided onapparatus 10 or alternatively may be provided as a separate system andfluidly connected to the chamber.

RIE apparatus 10 also includes a fluid feeder, preferably in the form ofa mass flow controller that regulates the fluid used to create the thinfilm, the fluid being pumped into the chamber after evacuation thereof.The feeder may be provided on apparatus 10 or alternatively may beprovided as a separate system and fluidly connected to the chamber. Thefeeder supplies fluid in the proper volumetric rate or mass flow rate tothe chamber during etching. The etching gases can include, for example,oxygen, argon, chlorine, fluorine, carbon tetrafluoride,carbontetrachloride, perfluoromethane, perfluoroethane,perfluoropropane, nitrogen trifluoride, sulfur hexafluoride, methane,and the like. Mixtures of gases may be used advantageously to enhancethe etching process.

RIE apparatus 10 also includes a power source electrically connected toelectrode 80 via electrical terminal 30. The power source may beprovided on apparatus 10 or alternatively may be provided on a separatesystem and electrically connected to the electrode via electricalterminal (as shown in FIG. 2). In any case, the power source is anypower generation or transmission system capable of supplying sufficientpower. (See discussion infra.)

Although a variety of power sources are possible, RF power is preferred.This is because the frequency is high enough to form a self bias on anappropriately configured powered electrode but not high enough to createstanding waves in the resulting plasma. RF power is scalable for highoutput (wide webs or substrates, rapid web speed). When RF power isused, the negative bias on the electrode is a negative self bias, thatis, no separate power source need be used to induce the negative bias onthe electrode. Because RF power is preferred, the remainder of thisdiscussion will focus exclusively thereon.

The RF power source powers electrode 80 with a frequency in the range of0.01 to 50 MHz preferably 13.56 MHz or any whole number (for example, 1,2, or 3) multiple thereof. This RF power as supplied to electrode 80creates a plasma from the gas within the chamber. The RF power sourcecan be an RF generator such as a 13.56 MHz oscillator connected to theelectrode via a network that acts to match the impedance of the powersupply with that of the transmission line (which is usually 50 ohmsresistive) so as to effectively transmit RF power through a coaxialtransmission line.

Upon application of RF power to the electrode, the plasma isestablished. In an 15 RF plasma the powered electrode becomes negativelybiased relative to the plasma. This bias is generally in the range of500 to 1400 volts. This biasing causes ions within the plasma toaccelerate toward electrode 80. Accelerating ions etch the article incontact with electrode 80 as is described in more detail below.

In operation, a full spool of substrate upon which etching is desired isinserted over the stem as spool 28A. Access to these spools is providedthrough lower door 18 since, in FIGS. 1 and 2, the spools are located inlower compartment 58 while etching occurs in upper compartment 56. Inaddition, an empty spool is fastened opposite the substrate holdingspool as spool 28B so as to function as the take-up spool after etchinghas occurred.

If a spacer web is desired to cushion the substrate during winding orunwinding, spacer web delivery and/or take-up spool can be provided asspools 28C and 28D (although the location of the spools in theparticular locations shown in the figures is not critical). Similarly,if etching is desired in a pattern or otherwise partial manner, amasking web can be positioned on an input spool as spool 28E and anempty spool is positioned as a take-up spool as spool 28F.

After all of the spools with and without substrates or webs arepositioned, the substrate on which etching is to occur (and any maskingweb to travel therewith around the electrode) are woven or otherwisepulled through the system to the take-up reels. Spacer webs generallyare not woven through the system and instead separate from the substratejust before this step and/or are provided just after this step. Thesubstrate is specifically wrapped around electrode 80 in channel 90thereby covering the exposed electrode portion. The substrate issufficiently taut to remain in contact with the electrode and to movewith the electrode as the electrode rotates so a length of substrate isalways in contact with the electrode for etching. This allows thesubstrate to be etched in a continuous process from one end of a roll tothe other. The substrate is in position for etching and lower door 18 issealed closed.

Chamber 24 is evacuated to remove all air and other impurities. Once anetchant gas mixture is pumped into the evacuated chamber, the apparatusis ready to begin the process of etching. The RF power source isactivated to provide an RF electric field to electrode 80. This RFelectric field causes the gas to become ionized, resulting in theformation of a plasma with ions therein. This is specifically producedusing a 13.56 MHz oscillator, although other RF sources and frequencyranges may be used.

Once the plasma has been created, a negative DC bias voltage is createdon electrode 80 by continuing to power the electrode with RF power. Thisbias causes ions to accelerate toward non-insulated electrode portion 90of electrode 80 (the remainder of the electrode is either insulated orshielded). The ions selectively etch the matrix material (versus thedispersed phase) in the length of substrate in contact with channel 90of electrode 80 causing anisotropic etching of the matrix material of onthat length of substrate.

For continuous etching, the take-up spools are driven so as to pull thesubstrate and any masking webs through the upper compartment 54 and overelectrode 80 so that etching of the matrix occurs on any unmaskedsubstrate portions in contact with annular channel 90. The substrate isthus pulled through the upper compartment continuously while acontinuous RF field is placed on the electrode and sufficient reactivegas is present within the chamber. The result is a continuous etching onan elongated substrate, and substantially only on the substrate. Etchingdoes not occur on the insulated portions of the electrode nor doesetching occur elsewhere in the chamber. To prevent the active power fedto the plasma from being dissipated in the end plates of the cylindricalelectrode, grounded dark space shields 86 and 88 can be used. Dark spaceshields 86 and 88 can be of any shape, size, and material that isconducive to the reduction of potential fouling. In the embodiment shownin FIGS. 1 and 2, dark space shields 86 and 88 are metal rings that fitover drum 26 and the insulation thereon. Dark space shields 86 and 88 donot bias due to the insulative material that covers drum 26 in the areaswhere dark space shields 86 and 88 contact drum 26. The dark spaceshields in this ring-like embodiment further include tabs on each endthereof extending away from drum 26 in a non-annular manner. These tabscan assist in aligning the substrate within channel 90.

Preferably, the temperature control system pumps fluid through electrode80 throughout the process to keep the electrode at a desiredtemperature. Typically, this involves cooling the electrode with acoolant as described above, although heating in some cases may bedesirable. In addition, since the substrate is in direct contact withthe electrode, heat transfer from the plasma to the substrate is managedthrough this cooling system, thereby allowing the coating of temperaturesensitive films such as polyethyleneterephthalate, polyethylenenaphthalate, and the like.

After completion of the etching process, the spools can be removed fromshafts supporting them on the wall. The substrate with thenanostructured article thereon is on spool 28B and is ready for use.

In some embodiments of the nanostructured articles of the invention, thenanostructured article comprise additional layers. For example, thearticle may comprise an additional fluorochemical layer to give thearticle improved water and/or oil repellency properties. Thenanostructured surface may also be post treated (for example, with anadditional plasma treatment). Plasma post treatments may include surfacemodification to change the chemical functional groups that might bepresent on the nanostructure or for the deposition of thin films thatenhance the performance of the nanostructure. Surface modification caninclude the attachment of methyl, fluoride, hydroxyl, carbonyl,carboxyl, silanol, amine, or other functional groups. The deposited thinfilms can include fluorocarbons, glass-like, diamond-like, oxide,carbide, nitride, or other materials. When the surface modificationtreatment is applied, the density of the surface functional groups ishigh due to the large surface area of the anisotropically etchednanostructured surface. When amine functionality is used, biologicalagents such as antibodies, proteins, enzymes, and the like can be easilygrafted to the amine functional groups. When silanol functionality isused, silane chemistries can be easily applied to the nanostructuredsurface due to the high density of silanol groups. Antimicrobial,easy-clean, and anti-fouling surface treatments that are based on silanechemistry are commercially available. Antimicrobial treatments mayinclude quaternary ammonium compounds with silane end group. Easy-cleancompounds may include fluorocarbon treatments such as perfluoropolyethersilane, hexafluoropropyleneoxide (HFPO) silane, and the like.Anti-fouling treatments may include polyethyleneglycol silane. When thinfilms are used, these thin films may provide additional durability tothe nanostructure or provide unique optical effects depending upon therefractive index of the thin film. Specific types of thin films mayinclude diamond-like carbon (DLC), diamond-like glass (DLG), amorphoussilicon, silicon nitride, plasma polymerized silicone oil, aluminum,copper, and the like.

The nanostructured articles of the invention can exhibit one or moredesirable properties such as antireflective properties, light absorbingproperties, antifogging properties, improved adhesion and durability.

For example, in some embodiments of the invention, the surfacereflectivity of the nanostructured anisotropic surface is about 50% orless than the surface reflectivity of an untreated surface. As usedherein with respect to comparison of surface properties, the term“untreated surface” means the surface of an article comprising the samematrix material and the same nanodispersed phase (as the nanostructuredsurface of the invention to which it is being compared) but without ananostructured anisotropic surface.

In some embodiments of the invention, the percent reflection of thenanostructured anisotropic surface is less than 2%, preferably, lessthan 1%, and most preferable less than 0.5%, as measured using the“Measurement of Average % Reflection” method described in the Examplesection below.

Likewise, in some embodiments of the invention, the percent transmissionof the nanostructured anisotropic surface is about 2% or more than thepercent transmission of an untreated surface as measured using the“Measurement of Average % Transmission” method described in the Examplesection below.

In other embodiments of the invention, the nanostructured anisotropicsurface has a water contact angle of less than about 20° (preferably,less than about 15°; more preferably less than about 10°) as measuredusing the “Water Contact Angle Measurement” method described in theExample section below.

In still other embodiments of the invention, the nanostructuredanisotropic surface absorbs about 2% or more light than an untreatedsurface.

In yet other embodiments of the invention, the nanostructuredanisotropic surface has a pencil hardness greater than about 2H(preferably, greater than about 4H) as determined according to ASTMD-3363-05.

Some embodiments of the invention further comprise a layer or coatingcomprising, for example, ink, encapsulant, adhesive, or metal attachedto the nanostructured anisotropic surface. The layer or coating can haveimproved adhesion to the nanostructured anisotropic surface of theinvention than to an untreated surface.

The nanostructured articles of the invention are useful for numerousapplications including, for example, display applications (for example,liquid crystal displays (LCD), light emitting diode (LED) displays, orplasma displays); light extraction; electromagnetic interference (EMI)shielding, ophthalmic lenses; face shielding lenses or films; windowfilms; antireflection for construction applications, constructionapplications or traffic signs; and the like. The nanostructured articlesof the invention are also useful for solar applications such as solarfilms and Fresnel lenses. They can be used as the front surface of solarthermal hot liquid/air heat panels or any solar energy absorbing device;for solar thermal absorbing surfaces having micro- or macro-columns withadditional nanoscale surface structure; for the front surface offlexible solar photovoltaic cells made with amorphous silicaphotovoltaic cells or CIGS photovoltaic cells; and for the front surfaceof a film applied on top of flexible photovoltaic cells.

FIG. 7 shows a schematic cross sectional view of an exemplary display100, such as a LCD, using an antireflective (AR) article as disclosedherein. In one embodiment, a composite 102 includes a substrate 104having opposing first and second surfaces with an AR layer 106 disposedon the first surface of the substrate and an optically clear adhesive(OCA) 108 disposed on the second surface of the substrate. Optionally arelease liner (not shown) can be used to protect the OCA and a premask(also not shown) can be used to protect the AR coating during processingand storage. The composite 102 is then laminated to a glass or polarizersubstrate 110 such that the OCA is in direct contact with the glasssubstrate which is then assembled to a liquid crystal module 112,typically, with an air gap 114 disposed between the AR coating and theliquid crystal module. The polymeric substrate, the OCA, and the ARlayer are further described below.

Suitable substrate for use in this present disclosure and particularlyfor display applications include any material that is at least 90%transmissible in visible light (400 to 800 nm wavelength) and has a hazeof less than about 5%. Illustrative examples of polymeric substratesinclude polycarbonate, poly(meth)acrylate, polyester, nylon, siloxane,fluoropolymer, urethane, epoxy, cyclic olefin copolymer, triacetatecellulose, diacrylate cellulose or blends or copolymers thereof, styrenebased polymers such as polystyrene, acrylonitrile-styrene copolymer, andolefin based polymers. In one embodiment, the substrate has a thicknessof up to 250 micrometer (μm). The substrate can contain a cross-linkablematerial selected from multi(meth)acrylate, polyester, epoxy,fluoropolymer, urethane, siloxane and blends and copolymers thereof.

The OCAs that may be used in the present disclosure are those thatexhibit an optical transmission of at least about 90%, or even higher,and a haze value of below about 5% or even lower, as measured on a 25 μmthick sample in the matter described below in the Example section underthe Haze and Transmission Testing for OCA. Suitable OCAs may haveantistatic properties, may be compatible with corrosion sensitivelayers, may be able to be released from the glass substrate bystretching the adhesive. Illustrative OCAs include those described inPCT International Publication Nos. WO 2008/128073 relating to antistaticoptically clear pressure sensitive adhesive and WO 2009/089137 relatingto stretch releasing OCA and U.S. Patent Application Publication Nos. US2009/0087629 relating to indium tin oxide compatible OCA; US2010/0028564 relating to antistatic optical constructions havingoptically transmissive adhesive and US 2010/0040842 relating toadhesives compatible with corrosion sensitive layers; and U.S.Provisional Patent Applications 61/036,501 relating to optically clearstretch release adhesive tape and 61/141,767 stretch release adhesivetape. In one embodiment, the OCA has a thickness of about 5 μm or less.

In one exemplary process the hardcoat, provided in liquid form, iscoated on to a first surface of the substrate. Depending on thechemistry of the hardcoat, the liquid is cured or dried to form a dry ARlayer on the substrate. The hardcoated substrate is then processedthrough the reactive ion etching (RIE) process described above using, inone exemplary method, the apparatus described in FIG. 1. In addition toexhibiting desirable properties including antireflective properties andantifogging properties described above, the RIE process also minimizesthe undesirable phenomenon of iridescence (also referred to as“interference fringes”). The difference between the refractive index ofthe substrate and the hardcoat layer can cause the phenomenon ofiridescence, which occurs when external light incident on the hardcoatlayer is reflected to produce rainbow-like colors. The iridescence ishighly undesirable in a display application as it will obstruct theimage on the display.

While some skilled in the art have tried to address the iridescence bymatching the refractive index between the substrate and coatingformulations, it is very challenging to provide a balanced performancebetween antireflection and iridescence with quarter wavelengthmultilayer coatings. In some embodiments of this disclosure, the RIEprocess can reduce the reflection from the air-front surface interfaceof the substrate coated with nanoparticle filled hardcoat, which in turnreduces the iridescence to achieve a layer exhibiting excellentantireflective properties and minimal iridescence. In other embodimentsof this disclosure, nanoparticles such as ZrO₂ can be used to tune therefractive index of coating matrix of the hardcoat to substantiallymatch that of the substrate. The resulted coated article after the RIEprocess disclosed herein exhibit excellent antireflective properties andminimal iridescence.

In another embodiment of the invention, the nanodispersed phase can beetched away using plasma to form a nanostructured (or nanoporous)surface. This method can be carried out using planar RIE or cylindricalRIE essentially as described above, but using etching selectivity tofavor etching the nanodispersed phase rather than the matrix (that is,by selecting gases that etch dispersed phase material rather than thematrix material).

EXAMPLES

Objects and advantages of this invention are further illustrated by thefollowing examples, but the particular materials and amounts thereofrecited in these examples, as well as other conditions and details,should not be construed to unduly limit this invention.

Plasma Treatment

The anisotropic nanostructures of this invention were obtained by usingthe plasma treatment system described in U.S. Pat. No. 5,888,594 (Davidet al.) with some modifications. The width of the drum electrode wasincreased to 14.5 (36.8 cm) and the separation between the twocompartments within the plasma system was removed so that all thepumping was carried out by means of the turbo-molecular pump and thusoperating at a much lower operating pressure than is conventionally donewith plasma processing.

Rolls of polymeric film were mounted within the chamber, the filmwrapped around the drum electrode and secured to the take up roll on theopposite side of the drum. The unwind and take-up tensions weremaintained at 3 pounds. The chamber door was closed and the chamberpumped down to a base pressure of 5×10⁻⁴ Torr. A gas mixture of eitherpure oxygen or argon combined with oxygen or perfluoropropane mixed withoxygen was introduced into the chamber under various conditionsdescribed in the examples below. The operating pressure was nominally 10mTorr. Plasma was turned on at a power of 2000 watts by applying radiofrequency power to the drum and the drum rotation initiated so that thefilm was transported at a desired speed stated in the followingexamples. Alternatively, pieces of polymeric film were taped around theedges on the drum electrode. The drum was rotated at a constant speedand plasma treatment was then done with different lengths of time.

Measurement of Average % Reflection

The average % reflection (% R) of the plasma treated surface wasmeasured using PerkinElmer Lambda 950 UV-VIS-NIR ScanningSpectrophotometer. One sample of each film was prepared by applyingYamato Black Vinyl Tape #200-38 (obtained from Yamato InternationalCorporation, Woodhaven, Mich.) to the backside of the sample. Clear poly(methyl methacrylate) (PMMA) film of which transmission and reflectionfrom both sides were predetermined was utilized to establish the %reflection from the black tape. The black tape was laminated to thebackside of the sample using a roller to ensure there were no airbubbles trapped between the black tape and the sample. To measure thefront surface total % reflection (specular and diffuse) by anintegrating sphere detector, the sample was placed in the machine sothat the non-tape side was against the aperture. The % reflection wasmeasured at an 8° incident angle and average % reflection was calculatedby subtracting the % reflection of the black tape for the wavelengthrange of 400-800 nm.

Measurement of Average % Transmission

The average % transmission was measured with an internally builtmachine. The machine uses a quartz tungsten halogen (QTH) lamp poweredwith a stabilized source and a custom 4″ (10.2 cm) Spectralon™ sphere asa light source to measure sample transmission using a D/0 geometry.There are two detectors: a Silicon CCD is used for the visible and nearinfrared (NIR), and an InGaAs diode array are used for the remainder ofthe NIR. A simple spectrograph with a Czerny-Turner optical layout and asingle grating is used for light dispersal onto each detector. Thisallows optical transmission measurement of film samples with incidentmeasurement angles varying between 0 degrees and 60 degrees over awavelength range of 380 nm to 1700 nm. The transmission was measured atnormal incident angle and average % transmission was calculated andreported for the wavelength range of 400-800 nm in the followingexamples.

Water Contact Angle Measurement

Water contact angle was measured with a static contact angle measurementdevice. The machine is equipped with a digital camera, automatic liquiddispensers, and sample stages allowing hands-free contact angle viaautomated placement of a drop of water. The drop shape is capturedautomatically and then analyzed via Drop Shape Analysis by a computer todetermine the static contact angle.

Haze and Transmission Testing for the OC Adhesive

A 25 micron thick sample of the OC adhesive was laminated to a 25 micronthick Melinex® polyester film 454 (from DuPont Company, Wilmington,Del.) in a manner so as to assure that no air bubbles are trappedbetween the film and the adhesive layer. A 75 mm by 50 mm plain microslide (a glass slide from Dow Corning, Midland, Mich.), that had beenwiped three times with isopropanol, was laminated to the adhesive sampleusing a hand roller to assure no air bubbles were trapped between theadhesive and the glass slide. The percent (%) transmission and haze weremeasured using a Model 9970 BYK Gardner TCS Plus Spectrophotometer (fromBYK Gardner, Columbia, Md.). The background measurement was made with asandwich of the Melinex® polyester film 454 and the glass slide. The %transmission and the haze of the adhesive sample were then obtaineddirectly on the film/adhesive/glass laminate in the spectrophotometer.

Example 1

40 wt % of 20 nm silica particles filled acrylic coating was preparedfrom Nalco 2327, SR444 (pentaerythritol triacylate), A-174(methacryloxypropyltrimethoxy silane), and Irgacure™ 184(photoinitiator) according to the method described in U.S. Pat. No.5,104,929 (Bilkadi). The coating formulation was then diluted withisopropyl alcohol (IPA) to form 50 wt % solution. The coating solutionwas then coated onto primed 2 mil PET film. The solution wassyringe-pumped into a coating die, and the coating was dried by passingthrough an oven set at 120° C. and then cured by a UV source. Theresulting cured coating was approximately 4 microns thick. The sampleswere treated by oxygen plasma with different treatment times (30, 60,90, 120, 150, and 180 seconds). The average % reflection was measuredand reported in Table 1. Significant reduction in reflection wasobtained for Samples 2-7 and 90 seconds treatment provided the bestreflection behavior.

TABLE 1 Reflection results of plasma treated samples of Example 1 Sample1 2 3 4 5 6 7 O₂ plasma 0 30 60 90 120 150 180 treatment (control) time(seconds) Average 4.58 1.42 1.18 1.04 1.36 1.69 1.95 % R (400-800 nm)

Example 2

SR295 (pentaerythritol tetraacrylate) (240 gm), SR238 (hexane dioldiacrylate) (240 gm) and SR506 (isobornyl acrylate) (120 gm) werecombined and mixed. 5 nm silica particle Nalco 2326 (400 gm) was chargedto a 1 qt jar. 1-methoxy-2-propanol (450 gm),3-(Methacryloyloxy)propyltrimethoxy silane (27.82 gm) and 5% Prostab5128 (hindered amine nitroxide inhibitor) in water (0.23 gm) were mixedtogether and added to colloidal dispersion while stirring. The jar wassealed and heated to 80° C. for 16 hr. The surface modified silicadispersion (1166 gm), resin mixture (70 gm) of SR295, SR238 and SR506,and 5% Prostab in water (058 gm) were combined and mixed. The water and1-methoxy-2-propanol were removed from the mixture via rotaryevaporation. This yielded a clear composition (184.6 gm) of SiO₂ resinmixture. The weight percent of modified silica in the formulation wasabout 60 wt %. Preparation of 20 nm silica particle concentrate was donewith the same procedure by replacing Nalco 2326 with Nalco 2327. Thenanoparticles filled resins were diluted with the mixture of SR295,SR238, and SR506 for various concentrations of silica nanoparticles inthe acrylic hardcoat formulations. The hardcoats were then applied toprimed 5 mil PET film with two different particle sizes (5 nm and 20 nm)and various concentrations (10%, 20%, 40% and 50% by weight) of silicananoparticles in the acrylic coating mixture according to Table 2.One-side plasma treatment was then done under various web speeds (10, 5,3.3, 2.5, 1.7 and 1.3 feet/min) corresponding to different treatmenttimes (30, 60, 90, 120, 150 and 180 seconds). The transmission spectrumof the one-side treated samples was measured and the average %transmission in the wavelength range of 400-800 nm was calculated andreported in Table 2 and corresponding transmission enhancement resultsare reported in Table 3 below.

TABLE 2 Transmission results of plasma treated samples of Example 2 Ave% Transmission from 400-800 nm After RIE 5 nm 20 nm O₂ C3F8—O2 SiO2 SiO2before (etching time, sec) (etching time, sec) Samples (wt %) (wt %) RIE30 60 90 120 150 180 30 60 90 8 49.75 0 90.0 91.0 91.5 92.0 92.2 92.692.8 90.5 90.8 91.0 9 39.8 0 89.9 91.3 92.2 92.7 92.9 93.1 92.9 90.791.2 91.6 10 19.9 0 89.8 92.2 92.9 93.1 93.0 92.8 92.6 91.5 92.3 92.6 119.95 0 89.8 92.6 93.1 93.0 92.8 92.6 92.6 92.0 92.8 92.9 12 0 49.75 89.892.6 93.1 92.9 92.8 92.6 92.2 92.3 92.8 92.9 13 0 39.8 89.9 92.7 93.193.1 92.9 92.7 92.2 92.1 92.7 92.8 14 0 19.9 89.9 93.1 93.1 93.0 92.892.6 92.4 92.5 93.0 93.0 15 0 9.95 91.1 94.4 94.5 94.5 94.0 93.9 93.693.8 94.5 94.2 Ave % Transmission from 400-800 nm After RIE C3F8—O2Ar—O2 (etching time, sec) (etching time, sec) Samples 120 150 180 30 6090 120 150 180  8 91.3 91.6 91.7 90.8 91.3 91.9 92.2 92.6 92.2  9 91.992.2 92.4 91.1 92.0 92.7 92.8 92.9 93.1 10 92.6 93.1 93.2 92.3 92.9 93.092.8 92.8 92.7 11 92.9 93.2 93.1 92.8 93.1 93.0 92.8 92.7 92.7 12 93.093.1 93.1 92.4 93.1 93.0 92.9 92.6 92.7 13 92.9 93.1 93.0 92.5 93.0 92.993.0 92.5 92.4 14 93.0 93.1 92.9 93.0 93.2 92.8 92.7 92.6 92.5 15 94.394.3 94.0 94.7 94.7 94.3 94.3 93.7 93.8

TABLE 3 Transmission enhancement (%) achieved by various treatments ofExample 2 Delta % Transmission after RIE (400-800 nm) 5 nm 20 nm O₂C3F8—O2 Ar—O2 SiO2 SiO2 (etching time, sec) (etching time, sec) (etchingtime, sec) Samples (wt %) (wt %) 30 60 90 120 150 180 30 60 90 120 150180 30 60 90 120 150 180 8 49.75 0 1.0 1.5 2.0 2.2 2.6 2.8 0.5 0.8 1.01.3 1.6 1.7 0.8 1.3 1.9 2.2 2.6 2.2 9 39.8 0 1.4 2.3 2.8 3.0 3.2 3.0 0.81.3 1.7 2.0 2.3 2.5 1.2 2.1 2.8 2.9 3.0 3.2 10 19.9 0 2.4 3.1 3.3 3.23.0 2.8 1.7 2.5 2.8 2.8 3.3 3.4 2.5 3.1 3.2 3.0 3.0 2.9 11 9.95 0 2.83.3 3.2 3.0 2.8 2.8 2.2 3.0 3.1 3.1 3.4 3.3 3.0 3.3 3.2 3.0 2.9 2.9 12 049.75 2.8 3.3 3.1 3.0 2.8 2.4 2.5 3.0 3.1 3.2 3.3 3.3 2.6 3.3 3.2 3.12.8 2.9 13 0 39.8 2.8 3.2 3.2 3.0 2.8 2.3 2.2 2.8 2.9 3.0 3.2 3.1 2.63.1 3.0 3.1 2.6 2.5 14 0 19.9 3.2 3.2 3.1 2.9 2.7 2.5 2.6 3.1 3.1 3.13.2 3.0 3.1 3.3 2.9 2.8 2.7 2.6 15 0 9.95 3.3 3.4 3.4 2.9 2.8 2.5 2.73.4 3.1 3.2 3.2 2.9 3.6 3.6 3.2 3.2 2.6 2.7

Example 3

Coating solutions made from the blend of MA0736 POSS™ molecules(available from Hybrid Plastics Inc., Hattiesburg, Miss.), CN991(aliphatic urethane acrylate from Sartomer, Exton, Pa.), CN2303(alkoxylated multifunctional acrylate oligomer from Sartomer),tetrahyhydrofurfuryl alcohol (TFHA) and Lucirin™ TPO-L (photoinitiator,available from BASF) were applied to primed PET film and cured by UVsource. The coated film was then treated with oxygen plasma for 90seconds. The % reflection was measured and reported with theformulations and treatment conditions in Table 4.

TABLE 4 Reflection results of plasma treated samples of Example 3Formulation (wt %) O2 plasma CN991/CN2303 treatment time Average % RSample CN991 (70:30) THFA MA0736 TPO-L (seconds) (400-800 nm) 16 0 88 100 2 90 3.37 17 0 87 10 1 2 90 2.89 18 0 85 10 3 2 90 2.65 19 0 83 10 5 290 2.03 20 0 81 10 7 2 90 1.44 21 0 78 10 10 2 90 1.01 22 0 73 10 15 290 0.9 23 0 68 10 20 2 90 0.73

Example 4

Imperm™ 103 is nylon MXD6 comprising 3 wt % nano-scale talc andcommercially available from Nanocor Inc. Film sample was prepared fromImperm 103 by melt extrusion process through a slot die and then treatedby Ar—O2 plasma corresponding to different treatment times (30, 60, and90 seconds). The % reflection was then measured and reported in Table 5.

TABLE 5 Reflection results of plasma treated samples of Example 4 Sample24 25 26 27 Ar—O2 plasma 0 (Imperm 103 control) 30 60 90 treatment time(seconds) Average % R 5.12 4.25 2.05 0.95 (400-800 nm)

Example 5

In this example, Sample #5 in Example 1 was further treated by applyinga perfluoropolyether-silane (EGC-1720 available from 3M Company)solution to the etched surface. The static contact angle andtransmission for Sample #1, Sample #5, and Sample #5 treated withEGC-1720 were measured. The results are reported in Table 6 below. Thecontact angle to water is shown to be adjustable from below 10 degreesto above 120 degrees.

TABLE 6 Transmission and water contact test results of the samples inExample 5 Average % H2O contact transmission angle Sample Comment(400-800 nm) (degree) 1 PET coated with coating from 90.5 71.8 Example 1(Sample #1 in Example 1) 5 Sample #5 in Example 1 93.5 9.8 28 Sample #5treated with 94.1 122.5 EGC-1720

Example 6

In this example, a substrate web containing microstructure (BrightnessEnhancement Film-BEF made from 37 wt % 20 nm silica particles filledcoating in U.S. Patent Application Publication 20080050560-A1) was usedto generate a nanostructure on top of the microstructure by plasmatreatment. For the etching treatment, oxygen gas was used with atreatment time of 90 seconds with the flow rate, pressure and powermaintained at 500 sccm, 8 mTorr and 2000 watts respectively. The percentreflection was measured. The average % reflection in the wavelengthrange of 400-800 nm is reduced from 2.2% to 1%, a 50% reduction in thesurface reflection.

Example 7

Two of the plasma etched samples of Example 2 above (10 wt %concentration of 20 nm silica particles etched at 60 and 180 seconds)were characterized by cross-sectional high resolution scanning electronmicroscope (HRSEM). The results are depicted in FIG. 5 (5 feet/min) and6 (1.3 feet/min). It is clear that the etching is anisotropic in the sub100 nm range. Several holes and pillars that are in the 10-50 nmdiameter range are in the order of 500 nanometers range for depth,leading to a 5:1 aspect ratio or greater. The hole marked as “A” in FIG.6 has a diameter of 27 nanometers and a depth of 480 nanometers whilethe pillar marked as “B” has a diameter of 18 nanometers and a depth of364 nanometers. The corresponding aspect ratio of these structuresapproaches about 20:1.

Example 8

A flexible solar absorbing sheet was prepared with an extrusionreplication process and subsequently treated with plasma etching of thestructured surface. Carbon filled thermoplastic polyurethane(URC7000-TC-1 available from PolyOne Corp, Cleveland, Ohio) was meltedwith an extruder and formed through an extrusion sheet die onto acasting roll perforated with an array of holes distanced about 3 mmapart with depths of 0.5 cm and diameters of 2 mm. The extruder had adiameter of about 3.2 cm, a screw speed of 80 rpm, and a risingtemperature profile from 100° C. to 250° C. The extrusion replicationcasting roll was the center roll of a 3 roll stack with a nip rollcapable of pushing the carbon filled polymer melt into the castingreplication tool roll at a pressure of 0.24 MPa. The extrusionreplication casting process was operated at a speed of 0.61meters/minute. Total thickness of the extrusion replicated cast sheetwas 1.1 cm with 1.0 cm high posts or columns and 0.1 cm thickness ofcontinuous base film. % Reflection of this opaque columnar structuredsheet was then measured to be 3.1% with a Lambda 950 spectraphotometer.Since the opaque structured sheet had no measurable light transmission,% Absorption was calculated to be 1-% R or 96.9% absorption.

The flexible solar absorbing sheet was then treated by plasma in anO₂—C₃F₈ atmosphere for 60 seconds. % Reflection of the plasma etchedopaque columnar structured sheet was measured to 1.4% with a Lambda 950spectraphotomer demonstrating a 55% reduction in surface reflections. %Absorption of the plasma etched columnar-structured solar absorptionsheet was calculated to be 98.6%.

Example 9

An article of this invention was prepared according to Example 1, Sample5, using oxygen plasma and an etching time of 120 seconds. The adhesionof the anisotropically etched random nanostructure was measured againsttwo different types of adhesives, a premium silicon adhesive and an“extra strength” acrylic adhesive. For comparison, an unetched sample ofthe hardcoated substrate as in Example 1 was used. A 180 degree peeltester was used to test the adhesion strength.

Test samples were cut into approximately 2-inch (5.1 cm) wide×6-inch(15.2 cm) long strip and two different types of tapes having the twodifferent adhesive types were used. The silicone adhesive tape is a1-inch (2.5 cm) wide Scotch™ Tape No. 8403 with a silicone adhesive andthe acrylic adhesive tape is an “Extra Strength” ¾-inch (1.9 cm) wideScotch™ Crystal Clear tape having a product number 34-8505-5627-4,available from 3M Company (St. Paul, Minn.).

The adhesive tape was attached to the test samples by rolling a 4-inch(10.2 cm) diameter roller having a weight of 450 grams onto thetape/sample sandwich. Peel measurements were taken at a speed of 12inches/min (30.5 cm/min) over a test length of 0.5 inches (1.3 cm) andthe average peel value over this distance was measured. Six differentmeasurements were made for each type of sample/adhesive combination andsummarized in Table 7. The average and standard deviation of the sixmeasurements are also shown in this table.

TABLE 7 Peel Measurements from Example 9 Silicone Adhesive Peel AcrylicAdhesive Peel Sample No. Strength, Ave lb/in Strength, lb/in Control-11.29 1.133333 Control-2 1.31 1.2 Control-3 1.32 1.24 Control-4 1.221.173333 Control-5 1.34 1.2 Control-6 1.39 1.186667 Control Ave 1.3116671.188889 Control Std. Dev 0.051451 0.032126 Etched-1 1.95 2.626667Etched-2 2.04 2.72 Etched-3 2 2.786667 Etched-4 1.95 2.653333 Etched-51.9 2.76 Etched-6 1.94 2.786667 Etched Ave 1.963333 2.722222 Etched Std.Dev 0.044969 0.062736

Example 10

Pencil hardness test according to ASTM D-3363-05 test method wasutilized to evaluate the surface hardness of Sample 4 in Example 1. Acomplete set of pencil gradings starts with the hardest—9H, 8H, 7H, 6H,5H, 4H, 3H, 2H, F, HB, B, 2B, 3B, 4B, 5B, 6B, 7B, 8B, and 9B (the latteris the softest pencil). To perform the test, a pencil is used to make aline about one inch long on the sample. If the pencil leaves a visiblescratch on the surface, then take the next soft pencil to repeat thetest. The number of the first pencil that does not leave a visible markis considered the “pencil hardness” rating of the surface. Sample 4 inExample 1 was found to be 4H by this test method.

Example 11

This example illustrates the use of an antireflective layer madeaccording to Example 2 incorporated into a LCD. In particular, thehardcoat of Example 2 with 5 nm silica naoparticle was coated at 10% byweight on to a first surface of a 2 mil PET film, which was previouslyprimed. The dried hardcoated PET film was subjected to one-sided plasmatreatment using a gas mixture of 25% argon, 75% oxygen with a treatmenttime of 60 seconds to yield an AR film. Table 8 below reports the datafor 3 samples of Example 11 compared to 3 samples of Control(“Untreated” hardcoated PET).

An OC adhesive, such as product number 8171, commercially available from3M Company, was laminated to a second surface of the 5 mil PET film,i.e., on the side opposite of the hardcoat using a hand laminator toyield a composite. This composite was then laminated to a glasssubstrate and assembled with a liquid crystal module to yield a liquidcrystal display that can be used for electronic applications, such asmobile handheld (MHH) device.

TABLE 8 Transmission data of treated and untreated AR film of Example 11Transmission Example 11 (%) Sample 1 95.6 Sample 2 95.5 Sample 3 95.5Average 95.5 Untreated 1 92.6 Untreated 2 92.7 Untreated 3 92.6 Average92.6

Example 12

This example illustrates the situation where the hardcoat composition ismade such that it substantially matches the refractive index of thesubstrate.

The hardcoat solution is made by blending ZrO₂ naoparticles madeaccording to U.S. Pat. Nos. 6,376,590 and 7,241,437 dispersed in apolyacrylate matrix on to a first surface of a 5 mil PET film, which waspreviously primed. The solution was syringe-pumped into a coating die,and the coating was dried by passing through an oven set at 120° C. andthen cured by a UV source. The resulting cured coating was approximately4 microns thick. The dried hardcoated PET film was subjected toone-sided plasma treatment using a gas mixture of 25% argon, 75% oxygenwith a treatment time of 90 seconds to yield an AR film. Table 9 belowreports the data for 3 samples of this example compared to 3 samples of“Untreated” hardcoated PET.

An OC adhesive, such as product number 8171, commercially available from3M Company, was laminated to a second surface of the 5 mil PET film,i.e., on the side opposite of the hardcoat using a hand laminator toyield a composite. This composite was then laminated to a glasssubstrate and assembled with a liquid crystal module to yield a liquidcrystal display that can be used for MHH device. In this particularexample, the refractive index (N_(D)) of the glass was 1.52, of the OCadhesive was 1.50, of the PET substrate was 1.57, and of the AR layerwas 1.57.

TABLE 9 Transmission data of treated and untreated AR film of Example 12Transmission Example 12 (%) Sample 1 96.1 Sample 2 96.5 Sample 3 96.5Average 96.4 Untreated 1 93.4 Untreated 2 93.9 Untreated 3 93.5 Average93.6

Tables 8 and 9 shows transmission data of samples of Examples 11 and 12of the present disclosure compared to samples of the untreatedhardcoated PET. There is about a 3% gain in transmission after thehardcoated PET has been processed plasma treated through the reactiveion etching process, which is a significant increase for displayapplications. Such increase in transmission allows for lower powerconsumption by the display device as less battery power is needed tolight the MHH device.

Example 13

Surface modified silica particles (20 nm) were prepared from Nalco 2327,A-174 (methacryloxypropyltrimethoxy silane), and 1-methoxy-2-propanolaccording to the method described in U.S. Pat. No. 5,104,929 (Bilkadi)to form 43.4 wt % A-174 functionalized silica particles in1-methoxy-2-propanol.

Thereafter, 2.998 grams of the modified silica solution was blended with5.21 grams CN120M50 (epoxy acrylate blended with acrylic resin) fromSartomer Co., Inc., Exton, Pa., 4.9 grams isopropyl alcohol and 0.06grams TPO-L (photoinitiator) to form a mixture. This mixture wastransferred to a glass bottle where it was mixed by manually shaking thecontents and then further mixed using a Stuart roller mixture operatingat room temperature.

After mixing, the material was coated on to a 0.005 inch primed PET filmusing a Meyer rod (#8 bar) coating device. The coated PET film was driedat room temperature inside a ventilated hood for 15 minutes. The coatedfilm was cured using a UV processor equipped with a D-Bulb under anitrogen atmosphere. The sample was then treated by oxygen plasma for 90seconds. After plasma treatment, the average % reflection was 0.61%which is significantly lower than the value for the untreated filmhaving an average percent reflection of 4.72%.

The complete disclosures of the publications cited herein areincorporated by reference in their entirety as if each were individuallyincorporated. Various modifications and alterations to this inventionwill become apparent to those skilled in the art without departing fromthe scope and spirit of this invention. It should be understood thatthis invention is not intended to be unduly limited by the illustrativeembodiments and examples set forth herein and that such examples andembodiments are presented by way of example only with the scope of theinvention intended to be limited only by the claims set forth herein asfollows.

We claim:
 1. A composite comprising: (a) a substrate having at least 90%transmission in visible light and less than 5% haze, the substratehaving opposing first and second surfaces; (b) a nanostructured articledisposed on the first surface of the substrate, the nanostructuredarticle comprising a matrix and a nanoscale dispersed phase, and havinga major surface that is only an exposed etched random nanostructuredanisotropic surface defined by nano-pillars or nano-columns comprisingthe matrix and nanoscale dispersed phase, wherein the nano-pillars andnano-columns are structural asperities having an aspect ratio of 5:1 orgreater, and wherein the nanostructured article has a length along anx-direction, a width along a y-direction, and a thickness along az-direction, wherein the nanoscale features comprise nano-pillarsgenerally in the z-direction, wherein a majority of the nano-pillars arecapped with physically exposed nanoscale dispersed phase from thenanoscale phase in the matrix; (c) an optically clear adhesive disposedon the second surface of the substrate, the optically clear adhesivehaving at least 90% transmission in visible light and less than 5% haze.2. A display for electronic application comprising the composite ofclaim 1 laminated to a glass substrate such that the optically clearadhesive contacts the glass substrate, or a polarizer and assembling thelaminates with a liquid display module.
 3. The composite of claim 1,wherein the matrix comprises a hardcoat comprising nanoparticles ofSiO₂, ZrO₂ and combinations thereof dispersed in a crosslinkable matrixcomprising multi(meth)acrylate, polyester, epoxy, fluoropolymer,urethane, siloxane, or blends or copolymers thereof.
 4. The composite ofclaim 1, wherein the nanoscale dispersed phase comprises nanoparticlesof SiO₂, ZrO₂, TiO₂, ZnO, Al₂O₃, calcium carbonate, magnesium silicate,indium tin oxide, antimony tin oxide, poly(tetrafluoroethylene), carbon,and combinations thereof.
 5. The composite of claim 4, wherein thenanoparticles having average particle size of less than about 100 nm. 6.The composite of claim 5, wherein the nanoparticles are surfacemodified.
 7. The composite of claim 1, wherein the matrix comprises apolymer selected from the group consisting of polycarbonate,poly(meth)acrylate, polyester, nylon, siloxane, fluoropolymer, urethane,epoxy, cyclic olefin copolymer, triacetate cellulose, diacrylatecellulose or blends or copolymers thereof.
 8. The composite of claim 1,wherein the matrix comprises an inorganic material selected from thegroup of silicon oxide and tungsten carbide.
 9. The composite of claim1, wherein the substrate comprises a cross-linkable material selectedfrom multi(meth)acrylate, polyester, epoxy, fluoropolymer, urethane,siloxane, or blends or copolymers thereof.
 10. The composite of claim 1,wherein the substrate comprises a polymer selected from the groupconsisting of polycarbonate, poly(meth)acrylate, polyester, nylon,siloxane, fluoropolymer, urethane, epoxy, cyclic olefin copolymer,triacetate cellulose, diacrylate cellulose or blends or copolymersthereof.
 11. The composite of claim 1, wherein the substrate comprises aglass or a polarizer.
 12. The article of claim 1, wherein the matrixcomprises an alloy or a solid solution.
 13. The composite of claim 1,wherein the concentration of the dispersed phase within the matrix isbetween about 5 and 90 weight percent.